Allele Registry

Canonical Allele Identifier: PA916055728

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000013735

RCV001048768

RCV002284354

RCV002319419

RCV002513021

ClinVar Variation:

12875

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg188Trp	CA122767 NM_021007.3:c.562C>T